Diastereoselective formation of a dicopper(i) helicate with a chiral tetradentate pyridylthiazole ligand

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

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Detail(s)

Original languageEnglish
Pages (from-to)1999-2001
Journal / PublicationChemical Communications
Issue number15
Publication statusPublished - 2009

Abstract

Reaction of a pinene-based pyridylthioamide with 1,4-dibromo-2,3- butanedione in refluxing methanol yielded a new chiral pyridylthiazole ligand L which forms a dinuclear double-stranded helicate with Cu(i) ions; this helicate has opposite helical chirality when compared with its quaterpyridine analogue. © 2009 The Royal Society of Chemistry.

Citation Format(s)

Diastereoselective formation of a dicopper(i) helicate with a chiral tetradentate pyridylthiazole ligand. / Tsang, Chui-Shan; Yeung, Ho-Lun; Wong, Wing-Tak et al.
In: Chemical Communications, No. 15, 2009, p. 1999-2001.

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review